摘要
目的:研究脂联素基因T45G多态性与广东省一般人群非酒精性脂肪肝病(NAFLD)发病易感性的关系。方法:对正常对照组人群507例随访4年,基线和终点均进行问卷调查、体检、血生化和B超检查,终点时人群分为NAFLD组(185例)与正常对照纽(322例),采用聚合酶链反应限制性片段长度法(PCR—RFLP)检测基因多态性,分析2组间基因型和等位基因的频率分布,用多因素Logistic回归分析新发脂肪肝的危险因素。结果:NAFLD组与正常对照组基因型(TT:47.57%US50.93%,TG:45.40%vs42.24%,GG:7.03%US6.83%)和等位基因(T:70.27%掷72.05%,G;29.73%US27.95%)差异无统计学意义(P〉0.05)。按体重指数(BMI)正常与否分层后,2组间3种基因型频率的分布差异也无统计学意义(P〉0.05)。结论:脂联素基因T45G多态性与NAFLD的发病易感性不相关。
Objective: To investigate the correlation between adiponectin gene T45G polymorphisms and susceptibility of non-alcoholic fatty liver disease(NAFLD) in Guangdong Province. Methods: 507 normal control cases out of general population in Guangdong Province were prospectively followed-up for 4 years. Questionnaires, physical examination, blood biochemical tests and abdominal uhrasonography were carried out for each subject on the baseline and endpoint. The participants were divided into 2 groups at the endpoint : NAFLD (n = 185 ) and normal control( n = 322). Polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) was applied to detect the single nucleotide polymorphisms (SNPs). The genotype and allelic frequency distribution between 2 groups were analyzed. Multivariate regression logistic analysis was applied to identify the risk factors of incidental NAFLD. Results : The adiponectin genotypes (TT:47.57% vs 50.93% , TG:45.40% vs 42.24% , GG:7.03% vs 6. 83% )and allelic frequencies (T:70.27% vs 72.05%, G:29.73% vs 27.95% ) were not significantly different between NAFLD and normal control groups ( P 〉 0.05 ). When the participants were divided into two subgroups according to their BMI abnormality,the adiponectin genotypes were also not significantly different. (P 〉 0.05 ). Conclusion: The T45G polymorphisms of adiponectin gene were not shown to be associated with NAFLD susceptibility.
出处
《广州医学院学报》
2010年第2期1-5,共5页
Academic Journal of Guangzhou Medical College
基金
广州市卫生医药卫生科技重点项目(2008-ZDi-1)和(2009-ZDi-03).
关键词
非酒精性脂肪性肝病
脂联素基因
多态性
易感性
non-alcoholic fatty liver disease
adiponeetin gene
polymorphism
susceptibility